Canonical Allele Identifier: PA2825068333
Gene: GAMT HGNC NCBI

Linked Data

ClinVar Variation Id: 1098275

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000147.1:p.Gly61Arg
CA402997967
NM_000156.6:c.181G>C
CA402997969
NM_000156.6:c.181G>A